Evidence map›Paper›PMID 24440549›Full record

ArticleTuberculosis (Edinburgh, Scotland)2014

Role of the Mce1 transporter in the lipid homeostasis of Mycobacterium tuberculosis.

Marina Andrea Forrellad, Michael McNeil, María de la Paz Santangelo, Federico Carlos Blanco, Elizabeth García, Laura Inés Klepp, Jason Huff, Michael Niederweis, Mary Jackson, Fabiana Bigi

Open access · bronzeAbstract read
In one paragraph

Article in Tuberculosis (Edinburgh, Scotland), 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 53 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
53citing papers in PubMed, 1 pooled it
6.8field-weighted citation impact, top 2% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

53 citing papers in PubMed, 1 synthesis or guideline pooled it, 108 citations in OpenAlex.

  1. Pooled it
  2. Mce transport systems inJournal of bacteriology · 2026
    Review
  3. Article
  4. Article
  5. Article
  6. Antibiotic resistance inJAC-antimicrobial resistance · 2024
    Article
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  10. Article
  11. Article
  12. Review
  13. Article
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

10 authors at 2 institutions in 1 country.

Marina Andrea ForrelladInstituto de Biotecnología, CICVyA - INTA, N. Repetto and De los Reseros, Hurlingham 1686, Argentina.
Michael McNeilMycobacteria Research Laboratories, Department of Microbiology, Immunology & Pathology, Colorado State University, Fort Collins, CO 80523-1682, USA.
María de la Paz SantangeloInstituto de Biotecnología, CICVyA - INTA, N. Repetto and De los Reseros, Hurlingham 1686, Argentina.
Federico Carlos BlancoInstituto de Biotecnología, CICVyA - INTA, N. Repetto and De los Reseros, Hurlingham 1686, Argentina.
Elizabeth GarcíaInstituto de Biotecnología, CICVyA - INTA, N. Repetto and De los Reseros, Hurlingham 1686, Argentina.
Laura Inés KleppInstituto de Biotecnología, CICVyA - INTA, N. Repetto and De los Reseros, Hurlingham 1686, Argentina.
Jason HuffDepartment of Microbiology, University of Alabama at Birmingham, 609 Bevill Biomedical Research Building, 845 19th Street South, Birmingham, AL 35294, USA.
Michael NiederweisDepartment of Microbiology, University of Alabama at Birmingham, 609 Bevill Biomedical Research Building, 845 19th Street South, Birmingham, AL 35294, USA.
Mary JacksonMycobacteria Research Laboratories, Department of Microbiology, Immunology & Pathology, Colorado State University, Fort Collins, CO 80523-1682, USA.
Fabiana BigiInstituto de Biotecnología, CICVyA - INTA, N. Repetto and De los Reseros, Hurlingham 1686, Argentina. Electronic address: fbigi@cnia.inta.gov.ar.
Colorado State University · USUniversity of Alabama at Birmingham · US

Funding

Deciphering the function of Mce proteins from Mycobacterium tuberculosisR01AI083084 · NIAID · NATIONAL INSTITUTE OF AGRICULTURE TECH · PI BIGI, FABIANA · 2009 to 2012
$348k
NIAID NIH HHS 1 R01 AI083084NIAID NIH HHS R01 AI083084
6 · The paper itself

Abstract

Tuberculosis is one of the leading causes of mortality throughout the world. Mycobacterium tuberculosis, the causative agent of human tuberculosis, has developed several strategies involving proteins and other compounds known collectively as virulence factors to subvert human host defences and invade the human host. The Mce proteins are among these virulence-related proteins and are encoded by the mce1, mce2, mce3 and mce4 operons in the genome of M. tuberculosis. It has been proposed that these operons encode ABC-like lipid transporters; however, the nature of their substrates has only been revealed in the case of the Mce4 proteins. Here we found that the knockout of the mce1 operon alters the lipid profile of M. tuberculosis H37Rv and the uptake of palmitic acid. Thin layer chromatography and liquid chromatography-mass spectrometry analysis showed that the mce1 mutant accumulates more mycolic acids than the wild type and complemented strains. Interestingly, this accumulation of mycolic acid is exacerbated when bacteria are cultured in the presence of palmitic acid or arachidonic acid. These results suggest that the mce1 operon may serve as a mycolic acid re-importer.

Indexed as

Antigens, BacterialBacterial ProteinsFemaleGene Expression Regulation, BacterialHomeostasisHumansHydrolasesLipid MetabolismMaleMycolic AcidsOperonSequence Analysis, DNATuberculosisAntigens, BacterialBacterial ProteinsHsaD protein, Mycobacterium tuberculosisHydrolasesmammalian cell entry protein Mce1A, Mycobacterium tuberculosisMycolic AcidsLipidsmce operonMycobacterium tuberculosisMycolic acid

Identifiers

PMID24440549
PMCPMC3951760
OpenAlexW2016538712

What OpenQuestion holds

Textmetadata
LicenceTDM
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.